A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16903277



Internal ID2998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3900758..3916505hg38UCSC Ensembl
chr1:3817322..3833069hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3815748
hg1915748
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427829
Supporting Variants
Samples
Known GenesLINC01134
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16903277
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002811


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